Canonical Allele Identifier: CA412891944

Gene: PQBP1

Linked Data

• MyVariant Identifiers: chrX:g.48760336C>A (hg19) ; chrX:g.48903059C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48903059C>A , CM000685.2:g.48903059C>A	GRCh38
NC_000023.10:g.48760336C>A , CM000685.1:g.48760336C>A	GRCh37
NC_000023.9:g.48645280C>A	NCBI36
NG_015967.1:g.10142C>A
NG_015968.2:g.91G>T
NG_034300.1:g.13900G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218224.9:c.773C>A	ENSP00000218224.4:p.Ala258Asp
ENST00000376563.6:c.773C>A	ENSP00000365747.1:p.Ala258Asp
ENST00000396763.6:c.773C>A	ENSP00000379985.1:p.Ala258Asp
ENST00000443648.6:c.773C>A	ENSP00000414861.2:p.Ala258Asp
ENST00000456306.2:c.164C>A	ENSP00000393013.2:p.Ala55Asp
ENST00000472742.6:c.*190C>A	ENSP00000509191.1:n.*190C>A
ENST00000474671.6:n.1928C>A
ENST00000477997.6:n.1722C>A
ENST00000486150.6:n.2028C>A
ENST00000692023.1:c.*1194C>A	ENSP00000509927.1:n.*1194C>A
ENST00000447146.7:c.773C>A MANE Select	ENSP00000391759.2:p.Ala258Asp
ENST00000651767.1:c.773C>A	ENSP00000498362.1:p.Ala258Asp
ENST00000218224.8:c.773C>A	ENSP00000218224.4:p.Ala258Asp
ENST00000247140.8:c.488C>A	ENSP00000247140.4:p.Ala163Asp
ENST00000376563.5:c.773C>A	ENSP00000365747.1:p.Ala258Asp
ENST00000376566.8:c.488C>A	ENSP00000365750.4:p.Ala163Asp
ENST00000396763.5:c.773C>A	ENSP00000379985.1:p.Ala258Asp
ENST00000447146.6:c.773C>A	ENSP00000391759.2:p.Ala258Asp
ENST00000463529.4:n.1119C>A
ENST00000465859.2:n.787C>A
ENST00000470059.5:n.987C>A
ENST00000470062.5:n.745C>A
ENST00000473764.5:n.1345C>A
ENST00000474671.5:n.833C>A
ENST00000477997.5:n.854C>A
NM_001032381.1:c.773C>A	NP_001027553.1:p.Ala258Asp
NM_001032382.1:c.773C>A	NP_001027554.1:p.Ala258Asp
NM_001032383.1:c.773C>A	NP_001027555.1:p.Ala258Asp
NM_001032384.1:c.773C>A	NP_001027556.1:p.Ala258Asp
NM_001167989.1:c.770C>A	NP_001161461.1:p.Ala257Asp
NM_001167990.1:c.749C>A	NP_001161462.1:p.Ala250Asp
NM_001167992.1:c.473C>A	NP_001161464.1:p.Ala158Asp
NM_005710.2:c.773C>A	NP_005701.1:p.Ala258Asp
NM_144495.2:c.488C>A	NP_652766.1:p.Ala163Asp
XM_005272571.3:c.770C>A	XP_005272628.1:p.Ala257Asp
XM_005272572.3:c.488C>A	XP_005272629.1:p.Ala163Asp
XM_011543884.1:c.773C>A	XP_011542186.1:p.Ala258Asp
XM_005272572.4:c.488C>A	XP_005272629.1:p.Ala163Asp
XM_011543884.2:c.773C>A	XP_011542186.1:p.Ala258Asp
XM_017029207.1:c.770C>A	XP_016884696.1:p.Ala257Asp
NM_001032381.2:c.773C>A	NP_001027553.1:p.Ala258Asp
NM_001032382.2:c.773C>A MANE Select	NP_001027554.1:p.Ala258Asp
NM_001032383.2:c.773C>A	NP_001027555.1:p.Ala258Asp
NM_001167989.2:c.770C>A	NP_001161461.1:p.Ala257Asp
NM_001167990.2:c.749C>A	NP_001161462.1:p.Ala250Asp
NM_144495.3:c.488C>A	NP_652766.1:p.Ala163Asp